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Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya

BACKGROUND: Gastrointestinal parasites are neglected infections, yet they cause significant burden to animal and human health globally. To date, most studies of gastrointestinal parasites focus on host-parasite systems that involve either a single parasite or a host species. However, when hosts shar...

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Autores principales: Obanda, Vincent, Maingi, Ndichu, Muchemi, Gerald, Ng’ang’a, Chege J., Angelone, Samer, Archie, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557494/
https://www.ncbi.nlm.nih.gov/pubmed/31181093
http://dx.doi.org/10.1371/journal.pone.0217929
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author Obanda, Vincent
Maingi, Ndichu
Muchemi, Gerald
Ng’ang’a, Chege J.
Angelone, Samer
Archie, Elizabeth A.
author_facet Obanda, Vincent
Maingi, Ndichu
Muchemi, Gerald
Ng’ang’a, Chege J.
Angelone, Samer
Archie, Elizabeth A.
author_sort Obanda, Vincent
collection PubMed
description BACKGROUND: Gastrointestinal parasites are neglected infections, yet they cause significant burden to animal and human health globally. To date, most studies of gastrointestinal parasites focus on host-parasite systems that involve either a single parasite or a host species. However, when hosts share habitat and resources, they may also cross-transmit generalist gastrointestinal parasites. Here we explore multi-host-parasite interactions in a single ecosystem to understand the infection patterns, especially those linked to livestock-wildlife interfaces and zoonotic risk. METHODS: We used both coprological methods (flotation and sedimentation; N = 1,138 fecal samples) and molecular identification techniques (rDNA and mtDNA; N = 18 larvae) to identify gastrointestinal parasites in nine sympatric host species (cattle, sheep, goats, wildebeest, Grant’s gazelles, Thomson’s gazelles, impala, vervet monkeys and baboons) in the Amboseli ecosystem, Kenya. RESULTS: We found that the host community harbored a diverse community of gastrointestinal helminths, including 22 species and/or morphotypes that were heterogeneously distributed across the hosts. Six zoonotic gastrointestinal helminths were identified: Trichuris spp., Trichostrongylus colubriformis, Enterobius spp. Oesophagostomum bifurcum, Strongyloides stercoralis and Strongyloides fuelleborni. The dominant parasite was Trichuris spp, whose ova occurred in two morphological types. Baboons were co-infected with Strongyloides fuelleborni and S. stercoralis. CONCLUSIONS: We found that the interface zone shared by wild ungulates, livestock and non-human primates is rich in diversity of gastrointestinal helminths, of which some are extensively shared across the host species. Closely related host species were most likely to be infected by the same parasite species. Several parasites showed genetic sub-structuring according to either geography or host species. Of significance and contrary to expectation, we found that livestock had a higher parasite richness than wild bovids, which is a health risk for both conservation and livestock production. The zoonotic parasites are of public health risk, especially to pastoralist communities living in areas contiguous to wildlife areas. These results expand information on the epidemiology of these parasites and highlights potential zoonotic risk in East African savanna habitats.
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spelling pubmed-65574942019-06-17 Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya Obanda, Vincent Maingi, Ndichu Muchemi, Gerald Ng’ang’a, Chege J. Angelone, Samer Archie, Elizabeth A. PLoS One Research Article BACKGROUND: Gastrointestinal parasites are neglected infections, yet they cause significant burden to animal and human health globally. To date, most studies of gastrointestinal parasites focus on host-parasite systems that involve either a single parasite or a host species. However, when hosts share habitat and resources, they may also cross-transmit generalist gastrointestinal parasites. Here we explore multi-host-parasite interactions in a single ecosystem to understand the infection patterns, especially those linked to livestock-wildlife interfaces and zoonotic risk. METHODS: We used both coprological methods (flotation and sedimentation; N = 1,138 fecal samples) and molecular identification techniques (rDNA and mtDNA; N = 18 larvae) to identify gastrointestinal parasites in nine sympatric host species (cattle, sheep, goats, wildebeest, Grant’s gazelles, Thomson’s gazelles, impala, vervet monkeys and baboons) in the Amboseli ecosystem, Kenya. RESULTS: We found that the host community harbored a diverse community of gastrointestinal helminths, including 22 species and/or morphotypes that were heterogeneously distributed across the hosts. Six zoonotic gastrointestinal helminths were identified: Trichuris spp., Trichostrongylus colubriformis, Enterobius spp. Oesophagostomum bifurcum, Strongyloides stercoralis and Strongyloides fuelleborni. The dominant parasite was Trichuris spp, whose ova occurred in two morphological types. Baboons were co-infected with Strongyloides fuelleborni and S. stercoralis. CONCLUSIONS: We found that the interface zone shared by wild ungulates, livestock and non-human primates is rich in diversity of gastrointestinal helminths, of which some are extensively shared across the host species. Closely related host species were most likely to be infected by the same parasite species. Several parasites showed genetic sub-structuring according to either geography or host species. Of significance and contrary to expectation, we found that livestock had a higher parasite richness than wild bovids, which is a health risk for both conservation and livestock production. The zoonotic parasites are of public health risk, especially to pastoralist communities living in areas contiguous to wildlife areas. These results expand information on the epidemiology of these parasites and highlights potential zoonotic risk in East African savanna habitats. Public Library of Science 2019-06-10 /pmc/articles/PMC6557494/ /pubmed/31181093 http://dx.doi.org/10.1371/journal.pone.0217929 Text en © 2019 Obanda et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Obanda, Vincent
Maingi, Ndichu
Muchemi, Gerald
Ng’ang’a, Chege J.
Angelone, Samer
Archie, Elizabeth A.
Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya
title Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya
title_full Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya
title_fullStr Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya
title_full_unstemmed Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya
title_short Infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in Kenya
title_sort infection dynamics of gastrointestinal helminths in sympatric non-human primates, livestock and wild ruminants in kenya
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557494/
https://www.ncbi.nlm.nih.gov/pubmed/31181093
http://dx.doi.org/10.1371/journal.pone.0217929
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